Abiotic stresses restrict the productivity and quality of agricultural crops. Glutathione S-transferase (GST) utilizes glutathione to scavenge reactive oxygen species (ROS) that result from abiotic stresses. This study aimed to determine the expression pattern of the MsGSTU8 gene and its effects on saline-alkali tolerance. MsGSTU8, from alfalfa (Medicago sativa ‘Zhaodong’), was transformed into transgenic tobacco (Nicotiana tabacum) and overexpressed to determine its effects on saline-alkali tolerance. The gene products in alfalfa localized to the cytoplasm and the transcript levels were higher in the leaves than the roots and stems. Expression was strongly induced by cold, drought, salt and saline-alkali stresses as well as abscisic acid (ABA) treatments. The transgenic tobacco lines had significantly higher transcription levels of the abiotic stress-related genes and higher GST activity than the wild types. Transgenic tobacco lines with saline-alkali treatments maintained their chlorophyll content, showed improved antioxidant enzyme activity and soluble sugar levels, reduced ion leakage, O2.−, H2O2 accumulation and malondialdehyde content. Our results indicate that overexpression of MsGSTU8 could improve resistance to saline-alkali stresses by decreasing the accumulation of ROS and increasing the levels of antioxidant enzymes. Furthermore, they suggest that MsGSTU8 could be utilized for transgenic crop plant breeding.
Plants regularly have to cope with abiotic stresses such as cold, heat, drought, salt and saline-alkali environments during their growth and development (Yu et al., 2018), which can seriously affect their yield and quality (Bechtold and Field, 2018; Shameer and Prasad, 2018). In the process of plant evolution, plants have developed various response mechanisms, especially molecular reaction pathways and regulatory networks, in order to adapt to abiotic stresses (Qu et al., 2013). Numerous induced genes have been identified in plants under abiotic stress, including heat shock proteins (Gruber et al., 2018; Traewachiwiphak et al., 2018; Zhao et al., 2018), transcription factors (Erpen et al., 2018; Klay et al., 2018; Moreno et al., 2018), protein kinases (Manuka et al., 2018; Ye et al., 2017; Zhou et al., 2018), protein phosphatases (Singh et al., 2010; Kong et al., 2018) and cellular protective enzymes (Hanaka et al., 2018; Suzuki et al., 2013). Glutathione S-transferases (GSTs; EC 188.8.131.52) are a group of multifunctional protective cellular enzymes found in all cellular organisms and are encoded by a large complex superfamily in plants (Abdul et al., 2018; Liu et al., 2017). GSTs affect the growth and development of plants through their involvement in plant primary metabolism, secondary metabolism, stress tolerance (Horváth et al., 2019; Kumar and Trivedi, 2018; Yang et al., 2019) and cell signal transduction. GSTs catalyze the nucleophilic addition of reduced glutathione hydrosulfuryl and lipophilic electrophilic substrates, including organic halides, epoxides, arene oxides, α-unsaturated carbonyls, β-unsaturated carbonyls, organic nitrate esters and organic thiocyanates. Solubility was increased by the conjugation of glutathione to such molecules, producing water-soluble products that facilitated further metabolic processing (Axarli et al., 2009). External toxins and endogenous toxic metabolites are isolated in vacuoles or transferred to the apoplast for degradation of conjugated substances by covalent bonding, reducing the toxicity of substrates (Edwards and Dixon, 2005; Flury et al., 1995; Marrs, 1996; Moons, 2003; Sandermann, 1992). GSTs act as binding proteins or ligands and can also function as non-enzyme carriers in intracellular transport and catalyze anthocyanin-glutathione binding following transport to the vacuole through a glutathione pump (Marrs, 1996). GST can scavenge reactive oxygen species (ROS) including superoxide anions, hydroxyl radicals, alkoxys and hydrogen peroxide to protect the organism from oxidative damage (Cummins et al., 1999). GSTs also play a vital role in the isoversion reaction, redox steady-state of cells and regulation of cellular program senescence (Moons, 2005). Based on sequence similarity, immunological reactivity, kinetic properties and structural conformation, GSTs have been found to be widespread among plants.
In previous research, GST genes have been shown to be expressed in response to various abiotic stresses. For example, ROS content was reduced in transgenic tobacco overexpressing JrGSTU1 under cold stress (Yang et al., 2016), AtGSTU19 facilitated the maintenance of the ROS balance of cells of transgenic Arabidopsis by improving the activity of GST and other antioxidant enzymes that enhanced resistance to salt stress (Xu et al., 2015a), the transcriptional levels of MaGSTU2 and MaGSTU3 increased under drought stress (Wang et al., 2013), and overexpression of LeGSTU2 conferred tolerance to drought stress in transgenic Arabidopsis (Xu et al., 2015b). Members of the GST family have been reported in many different plants, but MsGSTs that resist saline-alkali stress have yet to be investigated. Exploration of the function of MsGSTU8 in response to saline-alkali stress would thus be of value to the scientific community.
Alfalfa (Medicago sativa L.), is a perennial high-quality forage legume that has received attention due to the positive impact its cultivation has on soil fertility (Gu et al., 2018; Seppänen et al., 2018). Medicago sativa ‘Zhaodong’, a cultivar local to northeast China, is tolerant to saline-alkali stress, and can grow on saline-alkali soils without negative effects. The transcriptome of alfalfa was sequenced under saline-alkali treatments in a previous study to explore its resistance genes (An et al., 2016). The data from the RNA-Seq showed that MsGSTU8 was one of the genes expressed with significant difference under the saline-alkali stress conditions, suggesting that this increase in expression is a response to the environmental stress.
In this study, the MsGSTU8 gene was isolated from alfalfa, and the expression pattern of MsGSTU8 was characterized under different conditions. The MsGSTU8 gene was transformed into tobacco for further analysis, and the functional characterization of the MsGSTU8 gene was verified. This research demonstrates a potential molecular mechanism for alfalfa stress-tolerance under saline-alkali conditions.
Isolation and characterization of the MsGSTU8 gene
The MsGSTU8 gene cloned from alfalfa had a complete open reading frame, 675 bp in length, encoding a polypeptide composed of 224 amino acid residues. The predictive analysis of MsGSTU8 showed a hydrophilic protein containing GST_N and GST_C_2 domains without transmembrane domains. The predicted molecular mass was 25.9 kDa and the isoelectric point (pI) was 5.64. The BLAST analysis indicated that the determined amino acid sequence of MsGSTU8 showed homology and high identity with the GST family members from other plant species; the highest identity (96%) was found with MtGST (XP_003623196.1). The phylogenetic tree of MsGSTU8 and its closely related members from other plant species are shown in Fig. 1.
The MsGSTU8 protein is localized in the cytoplasm
The subcellular localization of MsGSTU8 was investigated using the MsGSTU8 and green fluorescence protein (GFP) fusion proteins that were overexpressed in Arabidopsis protoplast. The original p16318-GFP was used as a control vector. Microscopic visualization revealed that GFP fluorescence from the fusion protein was only detected in the cytoplasm of the Arabidopsis protoplast cells, whereas the fluorescence in the control was observed in all parts of the cell. The results suggested that MsGSTU8 is a cytoplasm-localized protein (Fig. 2).
Expression pattern analysis of the MsGSTU8 gene in alfalfa
The expression pattern of MsGSTU8 in the root, stem and leaf of alfalfa was analyzed with qPCR under normal conditions (Fig. 3A). The results showed that the MsGSTU8 gene was expressed in different tissues and the highest expression levels were in the leaf. The MsGSTU8 gene was induced by the cold, drought, salt, saline-alkali and abscisic acid (ABA) treatments to varying degrees in the leaf and root after exposures of 0, 1, 3, 6, 12 and 24 h (Fig. 3B–F).
The MsGSTU8 gene confers enhanced tolerance to saline-alkali stress in transgenic tobacco
The transgenic tobacco lines were generated by Agrobacterium-mediated transformations; 28 positive transgenic lines were identified from 65 transformants with glufosinate-ammonium resistance and the expression levels for the MsGSTU8 gene were then detected. The results of the qPCR showed that the MsGSTU8 gene was expressed in all of the transgenic lines. L26, L27 and L37 were chosen for further characterization owing to their high transcription levels of MsGSTU8 (Fig. 4A). Leaf discs were used for the saline-alkali stress phenotype assay in vitro. Phenotypic observations showed that the leaf discs of wild type (WT) had greater chlorosis than the transgenic tobacco lines under 30 mM NaHCO3 (Fig. 5A). The relative chlorophyll content of WT was significantly lower than that of the transgenic tobacco lines (Fig. 5B) under saline-alkali conditions. This indicates that transgenic tobacco lines exhibited higher tolerance than WT to the saline-alkali treatment.
MsGSTU8 improves the activity of GST in transgenic tobacco lines
The GST activity in the WT was significantly lower than in the transgenic tobacco lines under normal conditions. Under saline-alkali stress, both WT and transgenic tobacco had increased GST activity, but the transgenic lines had the highest activity levels (Fig. 4B).
MsGSTU8 protein in tobacco reduces O2.− and H2O2 levels but elevates antioxidant enzyme activities after saline-alkali stress
Analysis of WT and transgenic tobacco lines showed that the accumulation of superoxide anion radical (O2.−) and hydrogen peroxide (H2O2) in the WT was more than in the transgenic tobacco lines after saline-alkali treatments (Fig. 6). The activities of superoxide dismutase (SOD), peroxidase (POD) and catalase (CAT) increased to greater extents in the transgenic tobacco than in the WT (Fig. 7).
MsGSTU8 in transgenic tobacco decreases ion leakage and MDA levels but increases soluble sugar content under saline-alkali stress
To gain an insight into the degree of damage to plant cell membranes after saline-alkali treatments, the ion leakage and malondialdehyde (MDA) content were determined. The levels were higher in the WT than the transgenic tobacco lines. The accumulation of soluble sugars in the transgenic tobacco lines were higher than in the WT (Fig. 8).
The expression pattern of stress-related genes under saline-alkali stress
In order to shed light on the molecular events associated with MsGSTU8 under saline-alkali stress conditions, we investigated the effect of these conditions on the expression of stress response genes. The transcript levels of three ROS detoxification genes (NtSOD, NtPOD and NtCAT) and six stress response genes (NtRD29A, NtERD and NtLTP4) and proline biosynthesis genes (NtP5CS, NtLEA5 and NtLEA14) in the WT and transgenic tobacco lines after saline-alkali stress treatments showed that the expression of stress-related genes in transgenic tobacco lines were significantly higher in comparison to the WT after the saline-alkali treatment (Fig. 9).
Abiotic stresses cause osmotic stress and ion toxicity that produces excessive ROS, these in turn cause oxidative stress in plants. GST is an abundant enzyme in plants encoded by an ancient and highly divergent gene superfamily with multiple functions that play active roles in the ROS scavenging pathways of plants. Previous studies have shown that overexpressing a GST gene can enhance the tolerance of transgenic plants to salt (Csiszár et al., 2014; Ji et al., 2010; Xu et al., 2015b; Zhang et al., 2018), cold (Huang et al., 2009; Roxas et al., 1997), drought (Ji et al., 2010; Lo Cicero et al., 2015; Xu et al., 2015b) and heavy metals (Dixit et al., 2011; Kumar et al., 2013); the common mechanism for the increased tolerance is reduction of oxidative damage. In previous studies, it has been widely shown that GSTs respond to salt stress and are also induced by other abiotic and biotic stresses; however, the function of GSTs in response to saline-alkali stresses were unknown. The plants were damaged by osmotic stress and ion toxicity under salt stress conditions. The same stress factors with the added influence of high-pH damage were exerted by saline-alkali stress (Yang et al., 2008). The production of several oxyradicals was caused by the high-pH stress and this changed the membrane lipid components and destroyed photosynthetic parts of the plant cells, resulting in more serious oxidative injury with saline-alkali stress than salt stress alone. The transcriptome data revealed that many of the genes in the GST family were induced by the saline-alkali stress and the MsGSTU8 gene was significantly upregulated. The existing research indicates that the expression of certain GST genes were induced by: cold (Lo Piero et al., 2005), heavy metal ions (Shigeoka et al., 2002), salt (Diao et al., 2011), polyethylene glycol (PEG), H2O2, methylviologen (MV), ABA, salicylic acid (SA), jasmonic acid (JA), 1-naphthylacetic acid (NAA), auxin (IAA), cytokinin (CTK) and herbicides and safeners (Deridder et al., 2002) to respond to abiotic and biotic stresses (Dean et al., 2005; Gonneau et al., 2010). The transcription levels of the MsGSTU8 gene were tested in alfalfa under cold, drought, salt and ABA treatments, and the expression of the MsGSTU8 gene was shown to significantly increase. This shows that the MsGSTU8 gene was induced by the stress treatments, and that the MsGSTU8 gene might be located at the crossing point of multiple abiotic stress response pathways. The expression patterns of the MsGSTU8 gene were analyzed in the different organs of alfalfa and were found to have their highest expression levels in the leaf. The results of subcellular localization showed that MsGSTU8 was located in the cytoplasm, indicating that MsGSTU8 probably catalyzed GSH and various toxic secondary metabolites or exogenous products produced by the plant itself in the cytoplasm, the compounds that were formed could be identified and transported across the membrane by the glutathione pump, and the conjugates were sent to the vacuoles of the plant leaves. The MsGSTU8 gene was transformed into tobacco to determine the molecular mechanisms of plant responses to saline-alkali stress; the transcription levels of the MsGSTU8 gene were relatively high in the transgenic tobacco lines, with L26, L27 and L37 having the highest levels. The results of the GST activity assay were consistent with the previous results of the transcription levels of the MsGSTU8 gene, and the GST activity of the transgenic lines were found to be higher than in the WT. The phenotype showed that the leaves of WT were all whitened, while only part of the transgenic tobacco leaves showed whitening. As in earlier studies, the chlorophyll content of the plants was reduced under saline-alkali stress (Sun et al., 2014a). The chlorophyll content of transgenic tobacco lines showed a smaller decrease than that in the WT, possibly illustrating that the absorption and transduction effect of luminous energy in transgenic lines was less inhibited, relatively. For the NaHCO3 treatment, the high concentration of Na+ replaces the Ca2+ of the plant cytomembrane, changing the cytomembrane structure and permeability and leading to electrolyte leakage that was used as an indicator of cytomembrane damage or injury under saline-alkali stress. The greater the damage to the cytomembrane system from stress, the greater the cytomembrane permeability and the higher the relative electrical conductivity (Tantau and Dörffling, 2010). The electrolyte leakage of the transgenic tobacco line leaves increased under saline-alkali stress, but at a significantly lower level than with the WT, indicating that saline-alkali stress resulted in a change in cytomembrane permeability. The damage to the transgenic tobacco line cytomembrane system was less than that to the WT, meaning that MsGSTU8 could enhance membrane stability under saline-alkali stress, consistent with previous studies (Sun et al., 2014b). Photosynthesis was inhibited in the plant cells, and the accumulation of a large number of intracellular electrons was caused by the inhibition of the photosynthetic chain, thereby forming ROS in the chloroplasts, mitochondria and peroxisome under saline-alkali stress. Mitochondrial and chloroplast structures were degraded by excessive accumulation of ROS, affecting the structure and physiological functions of the biological macromolecules in the organelles, disrupting the normal physiological and metabolic intracellular activities (Yang et al., 2016). The ROS included the singlet oxygen (1O2), O2.−, hydroxyl radicals (HO) and H2O2 (Choudhury et al., 2017; Finkel and Holbrook, 2000; Karuppanapandian et al., 2011). Excess ROS were removed by enhancing the activity of enzymes in the antioxidant enzyme system such as SOD, POD and CAT in plants under saline-alkali stress (Bu et al., 2012). The O2.− was proportioned into H2O2 and O2 by SOD which was the first line of defense against ROS; H2O2 was generated by O2 and H2O under the catalysis of POD, CAT and other antioxidant enzymes (Pandhair and Sekhon, 2006). In tomato leaves, O2.− and H2O2 were produced by increasing the NaHCO3 concentration and the O2.− and H2O2 accumulations were increased as processing time increased (Gong et al., 2013). In this study, O2.− and H2O2 content in the transgenic tobacco lines were lower than in the WT under saline-alkali stress; this illustrates that transgenic tobacco lines were subjected to lower oxidative damage. The activity of SOD, POD and CAT in endophyte-infected rice with saline-alkali resistance was higher than in endophyte-uninfected rice which was saline-alkali sensitive under a 20 mM NaHCO3 treatment (Bu et al., 2012). The SOD, POD and CAT activity of transgenic tobacco lines was relatively higher than in the WT under saline-alkali stress; the high antioxidant enzyme activity of transgenic tobacco lines could clear the excess O2.− and H2O2, maintain the balance of ROS and reduce the toxic effects of ROS by conferring tolerance to oxidative stress in the cells. The accumulation of excess ROS would cause membranous peroxidation in the cell. MDA is the end soluble product during the process of membrane lipid peroxidation, and higher content of MDA indicates more serious damage to the cell membrane system; the content of MDA is usually used as a measure of the extent of oxidative stress (Janero, 1990; Mckay and Mason, 1991). The overexpression of GsTIFY10a in alfalfa conferred enhanced saline-alkali tolerance with a smaller increase of MDA content in comparison with the non-transgenic alfalfa (Zhu et al., 2014). In this study, the transgenic tobacco lines had a smaller increase of MDA content compared to the WT after saline-alkali stress, indicating that MsGSTU8 can maintain an oxidation-reduction equilibrium in cells to improve tolerance to saline-alkali stress. The salt content was high in the saline-alkali soil, making water absorption through plant roots difficult due to the decline of soil osmotic potential. Plants retain water in cells by osmoregulation; micromolecule organic compounds such as soluble sugars, soluble proteins and proline are synthesized in plants. Plants resist abiotic stress by increasing the synthesis of soluble sugars; a higher content contributes to improved plant tolerance to stress (Rosa et al., 2009). In this study, the soluble sugar content of transgenic tobacco lines was significantly higher than that of the WT after saline-alkali treatment; showing that the accumulation of osmotic substances in transgenic tobacco enhanced tolerance to the saline-alkali stress. The transcriptional level of genes that encoded antioxidant enzymes and stress responsive genes were upregulated in transgenic tobacco lines under saline-alkali treatments; this indicated that the MsGSTU8 gene overexpression in transgenic tobacco promoted the rapid response of related genes.
In conclusion, this study identifies a glutathione S-transferase family gene in alfalfa. The MsGSTU8 gene was upregulated significantly under cold, drought, salt, saline-alkali and ABA stress treatments. The expression of the MsGSTU8 gene was highest in the leaf of alfalfa and located in the cytoplasm. MsGSTU8 overexpression with higher GST activity might reduce the ROS accumulation by increasing other antioxidant enzyme activities to improve osmotic regulation to relieve ROS damage; it also might influence the transcription levels of the antioxidative genes and various stress resistance-related genes in stress responsive pathways to participate in the elimination of redundant ROS in transgenic tobacco lines. The results suggest that the MsGSTU8 gene plays an important role in saline-alkali stress responses in ABA-related regulatory systems. The MsGSTU8 gene could be used as a potential candidate to determine the molecular mechanisms and tolerance pathways for saline-alkali stress in plants.
MATERIALS AND METHODS
Plant materials, growth conditions and stress treatments
Alfalfa (Medicago sativa L.) cultivar ‘Zhaodong’, known to have strong abiotic stress tolerance, was used in this study. The seeds were provided by the Institute of Animal Husbandry, Heilongjiang Province, China and germinated in a petri dish at room temperature for 48 h in dark conditions. After 48 h, sprouted seeds were moved into pots of vermiculite with half-strength Hoagland's solution. The seedlings were grown in an incubation room, with photoperiods of 16 h light and 8 h dark. For analysis of the MsGSTU8 gene expression patterns, plant organs of alfalfa, including the roots, stems and leaves, were taken from 4-week-old seedlings under normal conditions. The leaves and roots of 4-week-old seedlings were used for cloning and analyzing the expression patterns of MsGSTU8 at 0, 1, 3, 6, 12 and 24 h after cold (4°C), drought (400 mM mannitol), salt (300 mM NaCl), saline-alkali (100 mM Na2CO3: NaHCO3, 1: 2), and 100 μM ABA treatments.
Tobacco (Nicotiana tabacum ‘SR I’) seeds were surface-sterilized with sodium hypochlorite and germinated on petri dishes containing MS (Murashige and Skoog) medium (pH 5.8) solidified with 3% sucrose and 0.8% agar at 25°C. The germinating seedlings were transplanted into culture flasks with the same culture conditions. Four-week-old tobacco seedlings were used for subsequent genetic transformations.
RNA isolation and qPCR analysis
Total RNA was extracted from the roots, stems and leaves of alfalfa for analysis of the expression pattern of MsGSTU8. RNAprep Pure Plant Kit (TianGen Biotech, Beijing, China) was used to extract RNA that was reverse-transcribed into cDNA by the EasyScript One-Step gDNA Removal and cDNA Synthesis SuperMix (TransGen Biotech, Beijing, China). Quantitative real-time PCR (qPCR) was performed to determine the expression pattern of MsGSTU8 with the specific primer P1 in different organs of alfalfa under normal conditions and the leaves and roots of alfalfa were treated with cold, drought, salt, saline-alkali and ABA treatments at different time points, respectively. The MtActin gene was used as the endogenous control gene to normalize the expression between different samples. The qPCR was performed using an Applied Biosystems 7300 Real-Time PCR System (Applied Biosystems, Foster City, CA, USA) and quantified with the comparative 2−ΔΔCt method, as previously described, to calculate the fold change of gene transcript levels. Each experiment was independently repeated in triplicate. The primers used for qPCR are listed in Table S1.
Cloning and bioinformatics analysis of MsGSTU8 gene
Based on the previous data of the transcriptome, the MsGSTU8 gene was obtained from the cDNA of alfalfa under saline-alkali treatments as a template and gene-specific primer P2 (Table S1) was designed. A search of the NCBI website (https://www.ncbi.nlm.nih.gov/orffinder/) was performed with the nucleotide sequence to determine the amino acid sequence of the MsGSTU8 gene. The SMART website (http://smart.embl-heidelberg.de/) was used to identify the domains and motifs. Predictions of the transmembrane domains were carried out on the TMHMM Server v. 2.0 website (http://www.cbs.dtu.dk/services/TMHMM/). The ExPASy website (http://web.expasy.org/protparam/) was used to predict the theoretical pI, molecular weight and hydrophilicity or hydrophobicity of the protein. The BLAST website (https://blast.ncbi.nlm.nih.gov/Blast.cgi) was used to find regions of similarity between the MsGSTU8 and other biological amino acid sequences. The related sequences were downloaded from the NCBI website to construct a phylogenetic tree using the Clustal X2 and MEGA 6.0 programs (Tamura et al., 2011; Thompson et al., 1997).
Subcellular localization of MsGSTU8 protein assay
For GFP and MsGSTU8 co-expressing constructions, the full-length coding sequence of the MsGSTU8 gene without its termination codon was amplified using a suitable primer P3 (Table S1) and inserted into the BamHI digested p16318-GFP vector to generate p16318-MsGSTU8-GFP. The fusion vector was introduced into Arabidopsis mesophyll protoplasts with p16318-GFP as the negative control. Green fluorescence from the transiently expressed constructs was observed at 488 nm using a confocal laser scanning microscope (Carl Zeiss, Jena, Germany).
Generation of MsGSTU8 transgenic tobacco
MsGSTU8 was ligated with a plant binary expression vector digested by the restriction sites of SacI and PstI to generate the recombinant constructions under the control of the cauliflower mosaic virus (CaMV) 35S promoter (Sham and Aly, 2012) with bar (phosphinothricin acetyltransferase) as the screening-labeled gene. The recombinant plasmid was transformed into an Agrobacterium tumefaciens strain EHA105 by the freeze-thaw method. The transgenic tobacco lines were obtained with Agrobacterium-mediated leaf disc transformation as described in a previous report (Hannah et al., 2006). Seeds of the transgenic tobacco lines were sown on MS medium containing glufosinate-ammonium (Sigma-Aldrich) to screen for the positive transgenic lines based on the resistance provided by the phosphinothricin acetyltransferase gene. To further confirm positive transgenic lines, PCR amplification of MsGSTU8 with primer P4 (Table S1) was used, with the extracted genomic DNA as a template. The qPCR was used to investigate the transcript levels of MsGSTU8 of the WT and transgenic tobacco lines, the NtGAPDH gene was used as an endogenous control (Table S1).
Measurement of GST activity
The GST activity was assayed using Habig's method by spectrophotometry (Habig and Jakoby, 1981; Habig et al., 1974). The reactions contained 50 mM KPO4 (pH 6.5), 0.4 mM 1-chloro-2,4-dinitrobenzene (CDNB), 5 mM GSH, and variable aliquots of enzyme extract (25–50 μg). Reactions were initiated with the addition of the CDNB substrate in ethanol. Enzymatic formation of 2,4-dinitrophenyl-S-glutathione at 340 nm (E340=9.6 mM−1 cm−1) was monitored for 5 min using a spectrophotometer and corrected for non-enzymatic controls.
Evaluation of transgenic tobacco exposed to saline-alkali stress
For saline-alkali stress tolerance assays, the leaf discs of 4-week-old WT and transgenic tobacco lines were immersed in liquid half-strength MS medium (pH 5.8) solidified with 3% sucrose containing 30 mM NaHCO3 for 5 days to estimate relative chlorophyll content. The chlorophylls are fat-soluble compounds that can be extracted from living plant tissue by organic solvents. The equation for 80% acetone is based on the specific absorption coefficients of Mackinney to estimate the total chlorophyll content (Lichtenthaler, 1987).
Oxidative damage analysis
For comparing the saline-alkali stress tolerance between the tobacco lines, 4-week-old WT and transgenic tobacco seedlings at similar stages of growth were treated with half-strength Hoagland's solution containing 30 mM NaHCO3 for 7 days. The electrolyte/ion leakage was measured as previously described with slight modifications. Briefly, the collected leaf discs of seedlings were dipped in the deionized water at room temperature for 2 h with a vacuum pump, and the initial conductivity (C1) was measured. Then, the samples were boiled for 15 min and cooled to room temperature to measure conductivity (C2); both conductivities were measured using a conductivity meter. The relative electrolyte leakage was calculated using the formula: ion leakage=100×C1/C2 (Huang et al., 2010). The content of superoxide anion radicals (Nakajima et al., 2009) and H2O2 (Veljovic-Jovanovic et al., 2002) were measured as described in previous reports. The activity of SOD (Huang et al., 2010), CAT (Beers and Sizer, 1952) and POD (Zhao et al., 2017) were spectrophotometrically measured, which is based on the ability of antioxidant enzymes to digest corresponding substrates. The test solutions for analysis of MDA (Lutts et al., 1996) and soluble sugar content (Wei et al., 2014) were extracted from the tobacco samples, using the methodology described in previous reports.
Stress-related gene expression analysis
The expression of antioxidative genes (NtSOD, NtPOD and NtCAT) and stress response genes, including those responsive to dehydration (NtRD29A), early response to dehydration (NtERD), a lipid transfer protein-coding gene (NtLTP4), pyrroline-5-carboxylate synthetase (NtP5CS) and late embryogenesis abundant protein-coding genes (NtLEA5 and NtLEA14) were examined in 4-week-old WT and transgenic tobacco lines under saline-alkali stress treatments. The NtGAPDH gene was used as an internal control; the primers used for qPCR are listed in Table S1.
All experiments were performed with three biological replicates with the same conditions. The data analyses were conducted with a one-sample Student's t-test or one-way ANOVA and shown as the mean±s.d. Statistical significance of the different methods occurred when P<0.05.
The authors are grateful to Dan Wang, Lei Ling, Lu Tang and Wenrui Zhang for critical reading of the manuscript.
Conceptualization: B.D., L.S.; Methodology: B.D., Y.A., L.S.; Software: B.D., X.Z.; Validation: B.D., Y.L.; Formal analysis: B.D.; Investigation: Y.A., Y.L.; Resources: B.D., C.G.; Data curation: B.D., X.Z.; Writing - original draft: B.D.; Writing - review & editing: B.D., W.Z., L.S., C.G.; Visualization: Y.A.; Supervision: C.G.; Project administration: C.G.; Funding acquisition: B.D., C.G.
Funding for this study was provided by: the National Key Research and Development Program of China (2017YFD0101303); National Natural Science Foundation of China (31770575, 31470571); The National Major Project for Cultivation of Transgenic Crops (2016ZX08004-002-003); Programs for Science and Technology Development of Heilongjiang Provice, China (GA18B104); and Graduate Innovation Fund of Harbin Normal University (HSDBSCX2015-09).
The authors declare no competing or financial interests.